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Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Gan-Or, Ziv; Bouslam, Naima; Birouk, Nazha; Lissouba, Alexandra; Chambers, Daniel B; Vérièpe, Julie; Androschuk, Alaura; Laurent, Sandra B; Rochefort, Daniel; Spiegelman, Dan; Dionne-Laporte, Alexandre; Szuto, Anna; Liao, Meijiang; Figlewicz, Denise A; Bouhouche, Ahmed; Benomar, Ali; Yahyaoui, Mohamed; Ouazzani, Reda; Yoon, Grace; Dupré, Nicolas; Suchowersky, Oksana; Bolduc, Francois V; Parker, J Alex; Dion, Patrick A; Drapeau, Pierre; Rouleau, Guy A; Ouled Amar Bencheikh, Bouchra.
Affiliation
  • Gan-Or Z; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Human Genetics, McGill University, Montréal, QC H3A 0G4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Bouslam N; Equipe de Recherche sur les Maladies Neurodégénératives, Medical School and Pharmacy, Mohammed V University, Rabat, BP 6527, Morocco.
  • Birouk N; Service de Neurophysiologie Clinique, Hôpital des Spécialités, Centre Hospitalier Ibn Sina, Université Mohammed V Souissi, Rabat, BP 6527, Morocco.
  • Lissouba A; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada; Département de Pathologie et Biologie Cellulaire, Université de Montréal, Montréal, QC H3C 3J7, Canada.
  • Chambers DB; Department of Pediatrics, Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB T6G 2R3, Canada.
  • Vérièpe J; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada; Département de Pathologie et Biologie Cellulaire, Université de Montréal, Montréal, QC H3C 3J7, Canada.
  • Androschuk A; Department of Pediatrics, Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB T6G 2R3, Canada.
  • Laurent SB; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Rochefort D; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Spiegelman D; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Dionne-Laporte A; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Szuto A; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada.
  • Liao M; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada; Département de Pathologie et Biologie Cellulaire, Université de Montréal, Montréal, QC H3C 3J7, Canada.
  • Figlewicz DA; Schulich School of Medicine and Dentistry, Western University, London, ON N6A 5C1, Canada.
  • Bouhouche A; Equipe de Recherche sur les Maladies Neurodégénératives, Medical School and Pharmacy, Mohammed V University, Rabat, BP 6527, Morocco.
  • Benomar A; Equipe de Recherche sur les Maladies Neurodégénératives, Medical School and Pharmacy, Mohammed V University, Rabat, BP 6527, Morocco.
  • Yahyaoui M; Equipe de Recherche sur les Maladies Neurodégénératives, Medical School and Pharmacy, Mohammed V University, Rabat, BP 6527, Morocco.
  • Ouazzani R; Service de Neurophysiologie Clinique, Hôpital des Spécialités, Centre Hospitalier Ibn Sina, Université Mohammed V Souissi, Rabat, BP 6527, Morocco.
  • Yoon G; Division of Neurology, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
  • Dupré N; Division of Neurology, Centre Hospitalier Universitaire de Québec, and Faculty of Medicine, Laval University, Quebec City, QC G1V 0A6, Canada.
  • Suchowersky O; Division of Neurology, University of Alberta, Edmonton, AB T6G 2R3, Canada.
  • Bolduc FV; Department of Pediatrics, Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB T6G 2R3, Canada.
  • Parker JA; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada; Département de Neurosciences, Université de Montréal, Montréal, QC H3C 3J7, Canada.
  • Dion PA; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada.
  • Drapeau P; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada; Département de Pathologie et Biologie Cellulaire, Université de Montréal, Montréal, QC H3C 3J7, Canada.
  • Rouleau GA; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Human Genetics, McGill University, Montréal, QC H3A 0G4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 0G4, Canada. Electronic address: guy.rouleau@mcg
  • Ouled Amar Bencheikh B; Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Centre de Recherche, Centre Hospitalier de l'Université de Montréal, Montréal, QC H2X 0A9, Canada.
Am J Hum Genet ; 98(5): 1038-1046, 2016 May 05.
Article in En | MEDLINE | ID: mdl-27153400
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Axons / Calpain / Spastic Paraplegia, Hereditary / Genetic Predisposition to Disease / Motor Neurons Limits: Adult / Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2016 Type: Article Affiliation country: Canada
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Axons / Calpain / Spastic Paraplegia, Hereditary / Genetic Predisposition to Disease / Motor Neurons Limits: Adult / Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2016 Type: Article Affiliation country: Canada